4-fluoro-1-(3-fluoro-5-iodophenoxy)-2-methoxybenzene | 1351862-06-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 4-fluoro-1-(3-fluoro-5-iodophenoxy)-2-methoxybenzene
• 英文别名: 1-Fluoro-3-(4-fluoro-2-methoxyphenoxy)-5-iodobenzene
• CAS: 1351862-06-0
• 化学式: C₁₃H₉F₂IO₂
• 分子量: 362.115
• InChiKey: VMQOUMUABWPGED-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  4.3
• 重原子数：
  18
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-fluoro-1-(3-fluoro-5-iodophenoxy)-2-methoxybenzene 、 丙烯腈 在 bis-triphenylphosphine-palladium(II) chloride 、 三乙胺 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 2.0h， 生成 、 (E)-3-[3-fluoro-5-(4-fluoro-2-methoxyphenoxy)phenyl]prop-2-enenitrile
  参考文献：
  名称：

  Computationally-Guided Optimization of a Docking Hit to Yield Catechol Diethers as Potent Anti-HIV Agents

  摘要：

  A 5-mu M docking hit has been optimized to an extraordinarily potent (55 pM) non-nucleoside inhibitor of HIV reverse transcriptase. Use of free energy perturbation (PEP) calculations to predict relative free energies of binding aided the optimizations by identifying optimal substitution patterns for phenyl rings and a linker. The most potent resultant catechol diethers feature terminal uracil and cyanovinylphenyl groups. A halogen bond with Pro95 likely contributes to the extreme potency of compound 42. In addition, several examples are provided illustrating failures of attempted grafting of a substructure from a very active compound onto a seemingly related scaffold to improve its activity.

  DOI：

  10.1021/jm201134m
• 作为产物：
  描述：

  4-氟-2-甲氧基苯酚 在 盐酸 、 铁粉 、 potassium carbonate 、 氯化铵 、 sodium nitrite 作用下， 以 乙醇 、 水 、 二甲基亚砜 为溶剂， 反应 4.25h， 生成 4-fluoro-1-(3-fluoro-5-iodophenoxy)-2-methoxybenzene
  参考文献：
  名称：

  Computationally-Guided Optimization of a Docking Hit to Yield Catechol Diethers as Potent Anti-HIV Agents

  摘要：

  A 5-mu M docking hit has been optimized to an extraordinarily potent (55 pM) non-nucleoside inhibitor of HIV reverse transcriptase. Use of free energy perturbation (PEP) calculations to predict relative free energies of binding aided the optimizations by identifying optimal substitution patterns for phenyl rings and a linker. The most potent resultant catechol diethers feature terminal uracil and cyanovinylphenyl groups. A halogen bond with Pro95 likely contributes to the extreme potency of compound 42. In addition, several examples are provided illustrating failures of attempted grafting of a substructure from a very active compound onto a seemingly related scaffold to improve its activity.

  DOI：

  10.1021/jm201134m